Canonical Allele Identifier: CA405753109

Gene: IFNL3

Linked Data

• dbSNP Id: rs2074934049
• gnomAD v3: 19-39244485-G-C
• gnomAD v4: 19-39244485-G-C
• MyVariant Identifiers: chr19:g.39735125G>C (hg19) ; chr19:g.39244485G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244485G>C , CM000681.2:g.39244485G>C	GRCh38
NC_000019.9:g.39735125G>C , CM000681.1:g.39735125G>C	GRCh37
NC_000019.8:g.44426965G>C	NCBI36
NG_042193.1:g.5487C>G
NG_055295.1:g.9372C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.202C>G	ENSP00000481633.1:p.Leu68Val
ENST00000413851.3:c.190C>G MANE Select	ENSP00000409000.2:p.Leu64Val
ENST00000413851.2:c.190C>G	ENSP00000409000.2:p.Leu64Val
ENST00000613087.4:c.202C>G	ENSP00000481633.1:p.Leu68Val
NM_172139.2:c.190C>G	NP_742151.2:p.Leu64Val
XM_005258765.3:c.202C>G	XP_005258822.1:p.Leu68Val
XM_011526757.1:c.202C>G	XP_011525059.1:p.Leu68Val
NM_001346937.1:c.202C>G	NP_001333866.1:p.Leu68Val
NM_172139.3:c.190C>G	NP_742151.2:p.Leu64Val
NM_172139.4:c.190C>G MANE Select	NP_742151.2:p.Leu64Val
NM_001346937.2:c.202C>G	NP_001333866.1:p.Leu68Val